Application of bis-eugenol to a zinc oxide eugenol cement

被引:38
作者
Fujisawa, S
Kashiwagi, Y
Atsumi, T
Iwakura, I
Ueha, T
Hibino, Y
Yokoe, I
机构
[1] Meikai Univ, Sch Dent, Dept Oral Diag, Sakado, Saitama 3500283, Japan
[2] Meikai Univ, Sch Dent, Dept Oral Physiol, Sakado, Saitama 3500283, Japan
[3] Meikai Univ, Sch Dent, Dept Dent Mat, Sakado, Saitama 3500283, Japan
[4] Josai Univ, Fac Pharmaceut Sci, Sakado, Saitama 3500283, Japan
关键词
eugenol; bis-eugenol; ZOE cement; setting time; compressive strength; solubility and disintegration; cytotoxicity;
D O I
10.1016/S0300-5712(98)00056-6
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objectives: To assess the usefulness of dimerized eugenol (bis-eugenol) in dentistry, the physical properties of zinc oxide eugenol cement (ZOE) with bis-eugenol and the cytotoxicity of bis-eugenol were studied. Methods: Setting time, compressive strength, solubility and disintegration of ZOE cement with bis-eugenol according to the specifications of JDMAS315 were evaluated. The cytotoxicity of bis-eugenol and eugenol toward two different cell types, HGF (a primary culture of human gingival fibroblast) and HSG (a human epidermoid carcinoma cell line derived from a salivary gland) was evaluated by the MTT test and in terms of cell survival. Results. Addition of bis-eugenol to ZOE did not decrease the physical properties when employed at the ratio of 9:1 or 6:1 (liquid ND:bis-eugenol, w/w). Bis-eugenol was less toxic than eugenol in the cell culture tests. Conclusions: The results of this assay demonstrated that bis-eugenol is useful in ZOE. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:291 / 295
页数:5
相关论文
共 22 条
[1]   Cytotoxicity of photosensitizers camphorquinone and 9-fluorenone with visible light irradiation on a human submandibular-duct cell line in vitro [J].
Atsumi, T ;
Murata, J ;
Kamiyanagi, I ;
Fujisawa, S ;
Ueha, T .
ARCHIVES OF ORAL BIOLOGY, 1998, 43 (01) :73-81
[2]  
ATSUMI T, 1998, J DENT RES B, V77
[3]   Skin sensitization to eugenol and isoeugenol in mice: Possible metabolic pathways involving ortho-quinone and quinone methide intermediates [J].
Bertrand, F ;
Basketter, DA ;
Roberts, DW ;
Lepoittevin, JP .
CHEMICAL RESEARCH IN TOXICOLOGY, 1997, 10 (03) :335-343
[4]   RESPIRATORY INHIBITION OF ISOLATED RAT-LIVER MITOCHONDRIA BY EUGENOL [J].
COTMORE, JM ;
BURKE, A ;
LEE, NH ;
SHAPIRO, IM .
ARCHIVES OF ORAL BIOLOGY, 1979, 24 (08) :565-568
[5]   H-1 AND C-13 NMR-STUDIES OF THE INTERACTION OF EUGENOL, PHENOL, AND TRIETHYLENEGLYCOL DIMETHACRYLATE WITH PHOSPHOLIPID LIPOSOMES AS A MODEL SYSTEM FOR ODONTOBLAST MEMBRANES [J].
FUJISAWA, S ;
KADOMA, Y ;
KOMODA, Y .
JOURNAL OF DENTAL RESEARCH, 1988, 67 (11) :1438-1441
[6]  
FUJITA Y, 1966, NIHON KAGAKUKAISHI, V87, P110
[7]   In vitro evaluation of the cytotoxicity of pure eugenol [J].
Gerosa, R ;
Borin, M ;
Menegazzi, G ;
Puttini, M ;
Cavalleri, G .
JOURNAL OF ENDODONTICS, 1996, 22 (10) :532-534
[8]  
Hensten-Pettersen A, 1991, Int Dent J, V41, P265
[9]   INFLUENCE OF DENTIN ON THE PULPWARD RELEASE OF EUGENOL OR ACIDS FROM RESTORATIVE MATERIALS [J].
HUME, WR .
JOURNAL OF ORAL REHABILITATION, 1994, 21 (04) :469-473
[10]  
*JAP DENT MAT MAN, 1997, GUID BOOK, P461